δ Opioid Receptor Inverse Agonists and their In Vivo Pharmacological Effects

被引:3
|
作者
Hirayama, Shigeto [1 ,2 ]
Fujii, Hideaki [1 ,2 ]
机构
[1] Kitasato Univ, Sch Pharm, Lab Med Chem, Minato Ku, 5-9-1 Shirokane, Tokyo 1088641, Japan
[2] Kitasato Univ, Sch Pharm, Med Res Labs, Minato Ku, 5-9-1 Shirokane, Tokyo 1088641, Japan
关键词
delta Opioid receptor; Constitutive activity; Inverse agonist; Neutral antagonist; Anorectic effect; Short-term memory improving effect; Antitussive effect; PROTEIN-COUPLED RECEPTORS; CONSTITUTIVE ACTIVITY; HIGHLY POTENT; WILD-TYPE; ANTAGONIST; BINDING; NALTRINDOLE; IMPAIRMENT; DESIGN; MICE;
D O I
10.2174/1568026620666200402115654
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The discovery of delta opioid receptor inverse agonist activity induced by ICI-174,864, which was previously reported as an delta opioid receptor antagonist, opened the door for the investigation of inverse agonism/constitutive activity of the receptors. Various peptidic or non-peptidic delta opioid receptor inverse agonists have since been developed. Compared with the reports dealing with in vitro inverse agonist activities of novel compounds or lcnown compounds as antagonists, there have been almost no publications describing the in vivo pharmacological effects induced by a delta opioid receptor inverse agonist. After the observation of anorectic effects with the delta opioid receptor antagonism was discussed in the early 2000s, the short-term memory improving effects and antitussive effects have been very recently reported as possible pharmacological effects induced by a delta opioid receptor inverse agonist. In this review, we will survey the developed delta opioid receptor inverse agonists and summarize the possible in vivo pharmacological effects by delta opioid receptor inverse agonists. Moreover, we will discuss important issues involved in the investigation of the in vivo pharmacological effects produced by a delta opioid receptor inverse agonist.
引用
收藏
页码:2889 / 2902
页数:14
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